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Understanding the Molecular Circuitry of Cell Lineage Specification in the Early Mouse Embryo

机译:了解早期小鼠胚胎中细胞谱系规范的分子电路

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Pluripotent stem cells hold great promise for cell-based therapies in regenerative medicine. However, critical to understanding and exploiting mechanisms of cell lineage specification, epigenetic reprogramming, and the optimal environment for maintaining and differentiating pluripotent stem cells is a fundamental knowledge of how these events occur in normal embryogenesis. The early mouse embryo has provided an excellent model to interrogate events crucial in cell lineage commitment and plasticity, as well as for embryo-derived lineage-specific stem cells and induced pluripotent stem (iPS) cells. Here we provide an overview of cell lineage specification in the early (preimplantation) mouse embryo focusing on the transcriptional circuitry and epigenetic marks necessary for successive differentiation events leading to the formation of the blastocyst.
机译:多能干细胞在再生医学中对基于细胞的疗法具有广阔的前景。但是,对于了解和利用细胞谱系规范,表观遗传重编程以及维持和分化多能干细胞的最佳环境至关重要,这是这些事件如何在正常胚胎发生中发生的基础知识。早期的小鼠胚胎提供了一个出色的模型,可用于研究对细胞谱系定型和可塑性以及胚胎衍生的谱系特异性干细胞和诱导性多能干(iPS)细胞至关重要的事件。在这里,我们提供了早期(植入前)小鼠胚胎中细胞谱系规格的概述,重点在于转录回路和表观遗传标记,这些信号是导致胚泡形成的连续分化事件所必需的。

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